Annex: References for Table 2.2 – human mutations This annex contains the references cited in Table 2.2 on human mutations. References for Table 2.2 Brown, P., et al[removed]Familial Creutzfeldt-Jakob Disease in Chile - Gerstmann–Sträussler–Scheinker syndrome - Document - PDFSEARCH.IO - Document Search Engine

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	Annex: References for Table 2.2 – human mutations This annex contains the references cited in Table 2.2 on human mutations. References for Table 2.2 Brown, P., et al[removed]Familial Creutzfeldt-Jakob Disease in Chile Add to Reading List Open Document File Size: 13,11 KB Share Result on Facebook City Berlin / / Company Furukawa / New England Journal / Kindred / / Country Slovakia / United Kingdom / United States / Chile / / MedicalCondition Peripheral Neuropathy / Gerstmann-Sträussler-Scheinker Syndrome / Late-Onset Dementia / Gerstmann-Sträussler-Scheinker Disease / GerstmannSträussler Syndrome / Creutzfeldt-Jakob Disease / Gerstmann-Sträussler Scheinker Syndrome / CreutzfeldtJakob Disease / Familial Creutzfeldt-Jakob Disease / Disease / Inherited Creutzfeldt-Jakob Disease / Gertsmann-Sträussler-Scheinker Disease / Gerstmann-Sträussler Syndrome / Fatal Familial Insomnia / Dysautonomia / Prion Protein Gene Are Not Associated With CJD / Experimental Transmissible Mink Encephalopathy / Prion Disease / / Movie A.D. / / Organization National Academy of Sciences / New York Academy of Science / / Person Jakob Kindred / Gene Linked / / PublishedMedium Nature Genetics / Proceedings of the National Academy of Sciences / American Journal of Human Genetics / Nucleic Acids Research / British Medical Journal / New England Journal of Medicine / / Technology Neuroscience / Neurosurgery / Genotype / / SocialTag Rare diseases Medicine Neurodegenerative disorders Genetics Jewish surnames PRNP Gerstmann–Sträussler–Scheinker syndrome Creutzfeldt–Jakob disease Prion Transmissible spongiform encephalopathies